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METIMMOX-2: Metastatic pMMR/MSS Colorectal Cancer - Shaping Anti-Tumor Immunity by Oxaliplatin

Study acronym: METIMMOX-2
StatusActive, Not Recruiting
PhasePhase 2
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Primary completion date: Sep 30, 2025 to Jan 31, 2028 Trial status: Recruiting to Active, Not Recruiting · Completion date: Dec 30, 2027 to Mar 1, 2028 · Site details revised at 3 of 3 sitesv4 Show 3 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Completion date: Dec 30, 2027 to Mar 1, 2028
    • Site details revised at 3 of 3 sites
  2. Minor Primary completion date: Sep 1, 2025 to Sep 30, 2025 Completion date: Dec 31, 2027 to Dec 30, 2027v3 Show 1 more changeShow less
    • Completion date: Dec 31, 2027 to Dec 30, 2027
  3. Notable Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Sep 1, 2022 to Oct 5, 2022 · Site details revised at 3 of 3 sites · Study description expanded, about 2 wordsv2 Show 3 more changesShow less
    • Start date changed from estimate of Sep 1, 2022 to Oct 5, 2022
    • Site details revised at 3 of 3 sites
    • Study description expanded, about 2 words

    See this version in full on ClinicalTrials.gov ↗

  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Hypothesis: Patients with metastatic colorectal cancer with DNA mismatch repair-proficient (pMMR) function / microsatellite-stable (MSS) phenotype harbor a non-immunogenic disease that can be transformed into an immunogenic condition by short-course oxaliplatin-based therapy, and may achieve durable disease control or even tumor eradication by the addition of immune checkpoint blockade therapy to the standard-of-care oxaliplatin-based treatment.
Trial Details
NCT Number NCT05504252
Lead Sponsor University Hospital, Akershus
Collaborators: Oslo University Hospital, St. Olavs Hospital
Conditions Colorectal Adenocarcinoma, Mucinous Adenocarcinoma, Signet Ring Cell Adenocarcinoma
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov